Canonical Allele Identifier: CA401621848
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs2047009119
gnomAD v4: 17-82750627-C-T
MyVariant Identifiers: chr17:g.80708503C>T (hg19) chr17:g.82750627C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750627C>T , CM000679.2:g.82750627C>T GRCh38
NC_000017.10:g.80708503C>T , CM000679.1:g.80708503C>T GRCh37
NC_000017.9:g.78301792C>T NCBI36
NG_011721.1:g.3564C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.802C>T MANE Select ENSP00000300784.7:p.Pro268Ser
ENST00000300784.7:c.802C>T ENSP00000300784.7:p.Pro268Ser
NM_022158.3:c.802C>T NP_071441.1:p.Pro268Ser
XM_024450872.1:c.652C>T XP_024306640.1:p.Pro218Ser
NM_022158.4:c.802C>T MANE Select NP_071441.1:p.Pro268Ser
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Search 100 bp 3'